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Neurogenetics

Showing results (621-630 of 949) with videos related to

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Neurogenetics|February 24, 2007
Altered neurodevelopment associated with mutations of RSK2: a morphometric MRI study of Coffin-Lowry syndromeShelli R Kesler, Richard J Simensen, Kytja Voeller, et al.
Neurogenetics|March 3, 2007
Bioinformatic analysis of human CNS-expressed ion channels as candidates for episodic nervous system disordersJan Freudenberg, Ying-Hui Fu, Louis J Ptácek
Neurogenetics|March 6, 2007
A novel gene derived from a segmental duplication shows perturbed expression in Alzheimer's diseaseDimitrios Avramopoulos, Ruihua Wang, David Valle, et al.
Neurogenetics|March 22, 2007
Confirmation of region-specific patterns of gene expression in the human brainCarl Ernst, Adolfo Sequeira, Tim Klempan, et al.
Neurogenetics|March 14, 2007
Influence of CCR5-Delta32 genotype in Spanish population with multiple sclerosisD Otaegui, J Ruíz-Martínez, J Olaskoaga, et al.
Neurogenetics|December 1, 2006
Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymiaHaijun Chen, Christian von Hehn, Leonard K Kaczmarek, et al.
Neurogenetics|July 25, 2007
Robust quantification of the SMN gene copy number by real-time TaqMan PCRIlsa Gómez-Curet, Karyn G Robinson, Vicky L Funanage, et al.
Neurogenetics|July 5, 2006
Interaction between the dopamine D4 receptor and the serotonin transporter promoter polymorphisms in alcohol and tobacco use among 15-year-oldsM H Skowronek, M Laucht, E Hohm, et al.
Neurogenetics|November 15, 2006
A null mutation in VAMP1/synaptobrevin is associated with neurological defects and prewean mortality in the lethal-wasting mouse mutantArne M Nystuen, Jamie K Schwendinger, Andrew J Sachs, et al.
Neurogenetics|August 25, 2010
A FOXG1 mutation in a boy with congenital variant of Rett syndromeTangui Le Guen, Nadia Bahi-Buisson, Juliette Nectoux, et al.
Pageof 95

Showing results (621-630 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|February 24, 2007
Altered neurodevelopment associated with mutations of RSK2: a morphometric MRI study of Coffin-Lowry syndromeShelli R Kesler, Richard J Simensen, Kytja Voeller, et al.
Neurogenetics|March 3, 2007
Bioinformatic analysis of human CNS-expressed ion channels as candidates for episodic nervous system disordersJan Freudenberg, Ying-Hui Fu, Louis J Ptácek
Neurogenetics|March 6, 2007
A novel gene derived from a segmental duplication shows perturbed expression in Alzheimer's diseaseDimitrios Avramopoulos, Ruihua Wang, David Valle, et al.
Neurogenetics|March 22, 2007
Confirmation of region-specific patterns of gene expression in the human brainCarl Ernst, Adolfo Sequeira, Tim Klempan, et al.
Neurogenetics|March 14, 2007
Influence of CCR5-Delta32 genotype in Spanish population with multiple sclerosisD Otaegui, J Ruíz-Martínez, J Olaskoaga, et al.
Neurogenetics|December 1, 2006
Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymiaHaijun Chen, Christian von Hehn, Leonard K Kaczmarek, et al.
Neurogenetics|July 25, 2007
Robust quantification of the SMN gene copy number by real-time TaqMan PCRIlsa Gómez-Curet, Karyn G Robinson, Vicky L Funanage, et al.
Neurogenetics|July 5, 2006
Interaction between the dopamine D4 receptor and the serotonin transporter promoter polymorphisms in alcohol and tobacco use among 15-year-oldsM H Skowronek, M Laucht, E Hohm, et al.
Neurogenetics|November 15, 2006
A null mutation in VAMP1/synaptobrevin is associated with neurological defects and prewean mortality in the lethal-wasting mouse mutantArne M Nystuen, Jamie K Schwendinger, Andrew J Sachs, et al.
Neurogenetics|August 25, 2010
A FOXG1 mutation in a boy with congenital variant of Rett syndromeTangui Le Guen, Nadia Bahi-Buisson, Juliette Nectoux, et al.
Pageof 95